A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608369



Internal ID6648608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24667974..24668414hg38UCSC Ensembl
Innerchr6:24668024..24668364hg38UCSC Ensembl
Outerchr6:24667856..24668532hg38UCSC Ensembl
chr6:24668202..24668642hg19UCSC Ensembl
Innerchr6:24668252..24668592hg19UCSC Ensembl
Outerchr6:24668084..24668760hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38441
hg19441
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12229664, essv12229660, essv12229663, essv12229659, essv12229665, essv12229661, essv12229662
SamplesHG03558, HG02756, NA19457, HG02588, HG02470, NA18987, NA18965
Known GenesACOT13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608369
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer